Literature DB >> 3907365

Morphologic demonstration of cytoplasmic ASSAM-related antigenic substance (CASSAM) by an immunoperoxidase technique.

S Takeshita, K Higuchi, M Hosokawa, A Matsumura, K Higuchi, A Kohno, M Matsushita, T Yonezu, T Takeda.   

Abstract

Murine senile amyloid protein identified in the senescence-accelerated mouse (SAM) was called ASSAM, and the ASSAM-related antigenic substance was detected in the cytoplasm of hepatocytes, columnar epithelia of the small intestine, and epithelia of the proximal convoluted tubules of the kidney, with the use of an immunoperoxidase method. This substance, called CASSAM (cytoplasmic ASSAM-related antigenic substance), did not stain positively with Congo red nor fibril structure, as determined under an electron microscope. As the ASSAM (senile amyloid) deposition increased with advancing age, CASSAM observed in hepatocytes and columnar epithelia decreased both in SAM-P and SAM-R strains. In the liver of the SAM-P strain in particular, the incidence and intensity in deposition of ASSAM increased rapidly from 5 months of age; on the other hand, CASSAM observed in the hepatocytes decreased rapidly at about the same time. Cycloheximide-treated animals showed a significantly low concentration of SASSAM (serum ASSAM-related antigenic substance) and also a low incidence and intensity of CASSAM observed in the cytoplasm of the hepatocytes and epithelia of the small intestine. In colchicine-treated animals, SASSAM concentration was slightly lower, and the severity of CASSAM observed in the cytoplasm was slightly higher, in the liver and kidney, as compared with control values. CASSAM is assumed to be synthesized in the cytoplasm of the cell and to be secreted alone or in the lipoprotein form into the serum. This CASSAM or lipoprotein including CASSAM is perhaps a constituent of SASSAM (CASSAM is assumed to include apoSASSAM) and the hepatocytes and intestinal mucosal epithelia are possible production sites of apoSASSAM.

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Year:  1985        PMID: 3907365      PMCID: PMC1887912     

Source DB:  PubMed          Journal:  Am J Pathol        ISSN: 0002-9440            Impact factor:   4.307


  31 in total

Review 1.  Intracellular aspects of the process of protein synthesis.

Authors:  G Palade
Journal:  Science       Date:  1975-08-01       Impact factor: 47.728

2.  Colchicine inhibition of plasma protein release from rat hepatocytes.

Authors:  C M Redman; D Banerjee; K Howell; G E Palade
Journal:  J Cell Biol       Date:  1975-07       Impact factor: 10.539

3.  Murine amyloidosis: immunologic characterization of amyloid fibril protein.

Authors:  C Isersky; D L Page; P Cuatrecasas; R A DeLellis; G G Glenner
Journal:  J Immunol       Date:  1971-12       Impact factor: 5.422

4.  The unlabeled antibody enzyme method of immunohistochemistry: preparation and properties of soluble antigen-antibody complex (horseradish peroxidase-antihorseradish peroxidase) and its use in identification of spirochetes.

Authors:  L A Sternberger; P H Hardy; J J Cuculis; H G Meyer
Journal:  J Histochem Cytochem       Date:  1970-05       Impact factor: 2.479

5.  Casein-induced experimental amyloidosis. 2. Lymphocyte transformation in preamyloidotic and amyloidotic guinea pigs.

Authors:  A B Briccetti; E S Cathcart; A S Cohen
Journal:  Acta Pathol Microbiol Scand Suppl       Date:  1972

6.  Amyloid. 8. On strain variability in experimental murine amyloidosis.

Authors:  J S Ram; R A DeLellis; G G Glenner
Journal:  Proc Soc Exp Biol Med       Date:  1969-02

7.  Mouse amyloid protein AA: Homology with nonimmunoglobulin protein of human and monkey amyloid substance.

Authors:  N Eriksen; L H Ericsson; N Pearsall; D Lagunoff; E P Benditt
Journal:  Proc Natl Acad Sci U S A       Date:  1976-03       Impact factor: 11.205

8.  Amyloid protein SAA is associated with high density lipoprotein from human serum.

Authors:  E P Benditt; N Eriksen
Journal:  Proc Natl Acad Sci U S A       Date:  1977-09       Impact factor: 11.205

9.  The SJL/J mouse: a new model for spontaneous age-associated amyloidosis. I. Morphologic and immunochemical aspects.

Authors:  M A Scheinberg; E S Cathcart; J W Eastcott; M Skinner; M Benson; T Shirahama
Journal:  Lab Invest       Date:  1976-07       Impact factor: 5.662

10.  Murine amyloid protein AA in casein-induced experimental amyloidosis.

Authors:  M Skinner; T Shirahama; M D Benson; A S Cohen
Journal:  Lab Invest       Date:  1977-04       Impact factor: 5.662

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  3 in total

1.  Molecular cloning and nucleotide sequence of cDNA for murine senile amyloid protein: nucleotide substitutions found in apolipoprotein A-II cDNA of senescence accelerated mouse (SAM).

Authors:  T Kunisada; K Higuchi; S Aota; T Takeda; H Yamagishi
Journal:  Nucleic Acids Res       Date:  1986-07-25       Impact factor: 16.971

2.  Age-related changes in bone mass in the senescence-accelerated mouse (SAM). SAM-R/3 and SAM-P/6 as new murine models for senile osteoporosis.

Authors:  M Matsushita; T Tsuboyama; R Kasai; H Okumura; T Yamamuro; K Higuchi; K Higuchi; A Kohno; T Yonezu; A Utani
Journal:  Am J Pathol       Date:  1986-11       Impact factor: 4.307

3.  Metabolism of senile amyloid precursor and amyloidogenesis. Age-related acceleration of apolipoprotein A-II clearance in the senescence accelerated mouse.

Authors:  H Naiki; K Higuchi; T Yonezu; M Hosokawa; T Takeda
Journal:  Am J Pathol       Date:  1988-03       Impact factor: 4.307

  3 in total

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